Real‐world use and outcomes of dolutegravir‐containing antiretroviral therapy in HIV and tuberculosis co‐infection: a site survey and cohort study in sub‐Saharan Africa

Abstract Introduction Dolutegravir is being scaled up globally as part of antiretroviral therapy (ART), but for people with HIV and tuberculosis co‐infection, its use is complicated by a drug–drug interaction with rifampicin requiring an additional daily dose of dolutegravir. This represents a disadvantage over efavirenz, which does not have a major drug–drug interaction with rifampicin. We sought to describe HIV clinic practices for prescribing concomitant dolutegravir and rifampicin, and characterize virologic outcomes among patients with tuberculosis co‐infection receiving dolutegravir or efavirenz. Methods Within the four sub‐Saharan Africa regions of the International epidemiology Databases to Evaluate AIDS consortium, we conducted a site survey (2021) and a cohort study (2015–2021). The cohort study used routine clinical data and included patients newly initiating or already receiving dolutegravir or efavirenz at the time of tuberculosis diagnosis. Patients were followed from tuberculosis diagnosis until viral suppression (<1000 copies/ml), a competing event (switching ART regimen; loss to program/death) or administrative censoring at 12 months. Results In the survey, 86 of 90 (96%) HIV clinics in 18 countries reported prescribing dolutegravir to patients who were receiving rifampicin as part of tuberculosis treatment, with 77 (90%) reporting that they use twice‐daily dosing of dolutegravir, of which 74 (96%) reported having 50 mg tablets available to accommodate twice‐daily dosing. The cohort study included 3563 patients in 11 countries, with 67% newly or recently initiating ART. Among patients receiving dolutegravir (n = 465), the cumulative incidence of viral suppression was 58.9% (95% confidence interval [CI]: 54.3–63.3%), switching ART regimen was 4.1% (95% CI: 2.6–6.2%) and loss to program/death was 23.4% (95% CI: 19.7–27.4%). Patients receiving dolutegravir had improved viral suppression compared with patients receiving efavirenz who had a tuberculosis diagnosis before site dolutegravir availability (adjusted subdistribution hazard ratio [aSHR]: 1.47, 95% CI: 1.28–1.68) and after site dolutegravir availability (aSHR 1.28, 95% CI: 1.08–1.51). Conclusions At a programmatic level, dolutegravir was being widely prescribed in sub‐Saharan Africa for people with HIV and tuberculosis co‐infection with a dose adjustment for the drug–drug interaction with rifampicin. Despite this more complex regimen, our cohort study revealed that dolutegravir did not negatively impact viral suppression.


I N T R O D U C T I O N
Dolutegravir, an integrase strand transfer inhibitor (InSTI), is recommended as part of preferred antiretroviral therapy (ART) regimens for people with HIV (PWH) [1,2]. Globally, HIV treatment programs are transitioning from nonnucleoside reverse transcriptase inhibitors (NNRTIs) [3,4], such as efavirenz, to dolutegravir because of its superior efficacy and tolerability, and high genetic barrier to HIV drug resistance [5,6]. The recommendation for dolutegravir is also inclusive of patients with tuberculosis co-infection [1,2]. Tuberculosis is a leading cause of morbidity and mortality among PWH globally [7] and affected approximately 815,000 PWH in 2019, among whom more than 70% were in sub-Saharan Africa [8].
For patients with tuberculosis co-infection, the use of dolutegravir is complicated by a drug-drug interaction with rifampicin [9], which is part of the standard 6-month treatment regimen for drug-susceptible tuberculosis [10]. Rifampicin induces the expression of UDPglucuronosyltransferase 1A1 (UGT1A1) and cytochrome P450 3A4, resulting in increased metabolism of dolutegravir and subsequently reduced plasma concentrations [9,11,12]. The reduced dolutegravir plasma concentrations can be overcome by increasing dolutegravir dosing from 50 mg once daily to 50 mg twice daily, maintained for 2 weeks after the last dose of rifampicin [9,13,14]. The more complicated management of this interaction is a disadvantage over efavirenz, which has no major drug-drug interaction with rifampicin [15]. In the International Study of Patients with HIV on Rifampicin ING (INSPIRING) trial, twice-daily dolutegravir was safe and well-tolerated among PWH receiving rifampicin-containing tuberculosis treatment [16]. Except for this trial, the recommendation for dolutegravir among patients with tuberculosis co-infection is largely extrapolated from trials among PWH without tuberculosis [1,2,6].
We sought to (1) describe HIV clinic practices for prescribing concomitant dolutegravir and rifampicin and (2) characterize virologic outcomes among patients with tuberculosis coinfection receiving dolutegravir and make comparisons with patients receiving efavirenz.

M E T H O D S
The data for this study came from the International epidemiology Databases to Evaluate AIDS (IeDEA) consortium, which collects routine clinical data from HIV care and treatment sites in 44 countries across seven geographical regions. This study, which focused on the four sub-Saharan Africa regional cohorts (Central, East, Southern and West; Appendix S1: members of the contributing IeDEA regions), consisted of a cross-sectional site survey of HIV clinics and a patient-level cohort study. Institutional review boards in each country and regional data management centre provided ethical oversight and approved the use of de-identified patient data. Consent requirements for study participation were deferred to local institutional review boards.

Site survey
We developed a survey about site practices for prescribing concomitant dolutegravir and rifampicin (Appendix S2) and successfully piloted it at one site. The survey asked about routine practices in the clinic and the respondent was instructed to consult other staff as needed to answer the questions. From August through October 2021, the survey was completed in English or French by clinical or administrative staff via Research Electronic Data Capture (REDCap) [17,18]. We included 109 sites that reported prescribing dolutegravir in a multiregional site survey conducted in 2020 at 137 IeDEA sites in sub-Saharan Africa [19]. Sites were excluded from the analysis if they did not provide ART to patients with tuberculosis disease (i.e. referring them to other sites) or stated that dolutegravir was not being prescribed at their site.

Cohort study
The cohort study used patient-level data collected at sites during routine clinical encounters for HIV care, through point of care data entry directly into an electronic health record or on paper forms later extracted into local databases. Data were de-identified before being transmitted to regional data management centres for processing and harmonization using an established data exchange standard [20].

Inclusion and exclusion criteria
We included sites that had begun to prescribe dolutegravir and were in countries with national guidelines that recommended dolutegravir as part of the preferred first-line ART regimen, including among patients with tuberculosis coinfection. We included patients who were ≥15 years old at HIV care enrolment and had a diagnosis of active tuberculosis from 24 months before their site began to use dolutegravir until 12 months before their site's database closure date. A diagnosis of tuberculosis was defined as documentation of a clinician's diagnosis or a proxy diagnosis based on documentation of initiating the standard regimen of isoniazid, rifampicin, pyrazinamide and ethambutol (HRZE) for drug-susceptible tuberculosis [21]. Additional inclusion criteria were for patients already on ART to be receiving efavirenz or dolutegravir at the time of tuberculosis diagnosis and for ARTnaïve patients to initiate ART with efavirenz or dolutegravir within 2 months after tuberculosis diagnosis.
To reduce potential misclassification of ART regimen at tuberculosis diagnosis, we excluded patients with conflicting ART regimen start dates (e.g. same start date for efavirenz and dolutegravir), likely resulting from data entry errors, as well as patients with a documented change in ART regimen (e.g. from dolutegravir to efavirenz) within 1 month after their tuberculosis diagnosis. ART regimens were defined as firstand second-line regimens recommended by the World Health Organization (WHO) [1,2], consisting of an NNRTI, InSTI or protease inhibitor (PI) and dual-nucleoside/nucleotide reverse transcriptase inhibitor (NRTI) backbone.

Start of dolutegravir use at site
Historical efavirenz (H-EFV) Historical efavirenz (H-EFV)

Dolutegravir (DTG)
Contemporaneous efavirenz (C-EFV) = Start of follow-up: date of tuberculosis diagnosis (≥12 months before site database closure) = End of event-free follow-up: administrative censoring at 12 months after tuberculosis diagnosis

End of study
Start of study (24 months before start of site dolutegravir use) = Approximate end of tuberculosis treatment: 6 months after tuberculosis diagnosis

Measures
Our exposure was receiving either a dolutegravir-or efavirenz-containing regimen at the time of tuberculosis diagnosis or initiating ART with such a regimen within 2 months after tuberculosis diagnosis. Patients receiving efavirenz comprised the control groups for comparison with dolutegravir and were stratified by timing of tuberculosis diagnosis, either before the introduction of dolutegravir at their site (historical efavirenz, "H-EFV") or after the introduction of dolutegravir at their site (contemporaneous efavirenz, "C-EFV") ( Figure 1). The inclusion of the H-EFV group allowed for a comparison when dolutegravir was not yet prescribed, potentially minimizing selection bias versus the comparison with the C-EFV group. Our outcome was viral suppression, which was defined as the earliest documentation of a viral load (VL) measurement <1000 copies/ml during follow-up. VL was based on documentation of a quantitative HIV RNA test using local site protocols and procedural standards. A threshold of 1000 copies/ml was chosen to reflect variation across sites in specimens used and assay lower limits of detection. Based on site testing capacity [22], we assumed that most patients would have VL ascertained during follow-up, and based on WHO guidelines [23], most would have one measurement, with multiple measurements among those with an unsuppressed VL.
Competing events were switching to a new ART regimen and loss to program or death, as these events could either modify the risk or prevent the occurrence of the viral suppression outcome. Switching to a new ART regimen was based on medication records, indicating the discontinuation of efavirenz or dolutegravir, that is switch from efavirenz to dolutegravir, a PI or another NNRTI, or switch from dolutegravir to an NNRTI or a PI. Reasons for regimen switches were not documented but were likely related to issues specific to the patient (e.g. tolerability) or program (e.g. antiretroviral availability). Loss to program included loss to follow-up (i.e. no record for ≥6 months immediately before administrative censoring at 12 months after tuberculosis diagnosis), known facility transfer or other documented reason for leaving care, with the last recorded date of contact used to determine the timing of this outcome. Determination of death was based on a site's usual practices for ascertainment.
Baseline variables were age group, sex, underweight (i.e. body mass index <18.5; based on measured height and weight closest to the date of tuberculosis diagnosis), documentation of a prior AIDS diagnosis (i.e. CD4 count <200 cells/mm 3 or CD4 + percentage <14, or WHO Clinical Stage 4 event), initial NRTI backbone, time of ART initiation, CD4 count closest to date of tuberculosis diagnosis (within 12 months before or 2 months after), most recent VL in the previous 12 months among those on ART for >6 months at tuberculosis diagnosis and site of tuberculosis disease (i.e. pulmonary only, extrapulmonary or unknown due to a proxy diagnosis). Documentation of an HRZE regimen included both patients with a proxy diagnosis and patients who initiated HRZE within 1 month of a documented tuberculosis diagnosis. As the collection and completeness of data on tuberculosis medications varied by site, we limited this variable to sites with ≥1 patient documented to receive HRZE.

Statistical analysis
For the site survey, we computed frequencies and proportions of all variables. For the cohort study, we computed descriptive statistics for patient characteristics and variables pertaining to data availability, overall and stratified by exposure group, and used Pearson's chi-squared tests (categorical variables) and Mann-Whitney U tests (numeric variables) to compare DTG with C-EFV and H-EFV. Patients were followed from their date of tuberculosis diagnosis until documentation of viral suppression, a competing event (i.e. switching ART regimen, loss to program or death) or administrative censoring at 12 months after tuberculosis diagnosis. If the viral suppression outcome was documented on the same day as a competing event, the patient was considered to have the former outcome.
We computed crude cumulative incidence proportions with 95% confidence intervals (CIs) for viral suppression and competing events using the Aalen-Johansen estimator [24]. We used multivariable Fine-Gray subdistribution hazards regression models [25] to estimate hazard ratios for viral suppression, comparing DTG with C-EFV and H-EFV. For each comparison, covariables in the model were patient characteristics that were significantly different between groups (p<0.05) in bivariate analyses, except for CD4 count, which was expected to be influenced by the decreasing use of CD4 testing over time [26]. In our assessment of viral suppression, we also stratified analyses by time of ART initiation, HRZE regimen documentation and site of tuberculosis disease. Cumulative incidence and regression analyses were conducted among the entire sample and among patients with VL ascertained in the 12 months after tuberculosis diagnosis. We conducted three sensitivity analyses: redefining viral suppression as <400 copies/ml; stratifying by the number of VL tests in the 12 months after tuberculosis diagnosis and by recent baseline VL among those initiating ART >6 months before tuberculosis diagnosis.

Site survey
Of 109 potentially eligible sites, 97 (89%) responded to the survey, of which seven were excluded because they referred patients with tuberculosis co-infection to other sites for management (n = 5) or did not use dolutegravir at their site (n = 2). The 90 sites that were included were in 18 countries, with 61 (69%) in an urban location and 47 (55%) with a primary level of care (Table S1).
Overall, 86 (96%) sites reported prescribing dolutegravir to PWH who were receiving rifampicin-containing tuberculosis treatment. Among these sites, routine practices regarding dolutegravir dosing varied: 69 (80%) reported that they start all patients on a second daily dose of dolutegravir, nine (10%) reported that all patients receive a once-daily dolutegravir regimen and eight (9%) reported that only some patients are started on a second daily dose. For the latter eight sites providing twice-daily dosing only to some patients, patient groups that do not routinely receive twice-daily dolutegravir include those with a history of adverse events or tolerability issues  related to ART (n = 5), those with low body weight (n = 4) and those at risk for suboptimal ART adherence (n = 1). Among the 77 sites that reported using twice-daily dosing, 74 (96%) reported having dolutegravir 50 mg tablets available on the day of the survey. Overall, four (4%) sites reported never prescribing dolutegravir to PWH who were receiving rifampicin-containing tuberculosis treatment. Of these sites, two reported routinely starting patients not yet on ART at the time of tuberculosis diagnosis on efavirenz-containing regimens. For patients already on dolutegravir at the time of tuberculosis diagnosis, the same two sites reported switching these patients to an efavirenz-containing regimen while receiving rifampicin. Practices at the other two sites were not ascertained. None of the four sites reported using other rifamycins.

Cohort study
Overall, 3636 patients met inclusion criteria of whom 73 were excluded, 44 for conflicting ART regimen start dates and 29 due to switching ART regimen within 1 month of tuberculosis diagnosis (Figure 2 Most patients (65%) were between 30 and 49 years old, 53% were male, 43% were underweight, 44% had a prior AIDS diagnosis and 67% initiated ART at the time of tuberculosis diagnosis or within 6 months prior (Table 1). Among those with a CD4 test (39%), the median count was 135 cells/mm 3 . Among patients on ART >6 months, 62% had a recent VL test, of whom 24% had a VL ≥1000 copies/ml. Most patients (61%) had a diagnosis of pulmonary only tuberculosis, 8% had a diagnosis of extrapulmonary tuberculosis and 32% had a proxy diagnosis. Among patients at sites reporting tuberculosis medications, 72% had documentation of HRZE.
Patients were categorized into the following exposure groups: DTG (n = 465), C-EFV (n = 702) and H-EFV (n = 2396). Overall, 93% were receiving an initial NRTI backbone of tenofovir plus lamivudine or emtricitabine, with no significant differences between DTG and EFV groups. Most patients in the DTG group were at sites that reported using twice-daily dolutegravir dosing with rifampicin (432 [93%]), eight (2%) were at sites reporting only once-daily dosing and 25 (5%) were at sites that did not participate in the survey.
When comparing patient characteristics of DTG with both EFV groups, there were significant differences in age group, sex and site of tuberculosis disease, and when comparing DTG with the H-EFV group, there were also significant differences in timing of ART initiation and CD4 count (Table 1). Compared with both EFV groups, patients in the DTG group were more often in older age groups (e.g. 26% vs. 16% ≥50 years), male (67% vs. 46-52%) and had documentation of pulmonary only tuberculosis (72% vs. 57-65%). Compared with H-EFV, patients in the DTG group less often initiated ART at the time of tuberculosis diagnosis (38% vs. 45%) and more often did so within 6 months prior (29% vs. 23%). CD4 counts were higher in the H-EFV group (median 142 cells/mm 3 ) versus DTG group (median 107 cells/mm 3 ); however, patients in the DTG group less often had a CD4 test (34% vs. 41%). Although ART-experienced patients in the DTG group were more likely than EFV groups to have a baseline VL test (81% vs. 59%), there were no significant differences in viral suppression. Documentation of HRZE was significantly lower in the DTG group (61%) compared with both EFV groups (73-75%).
At the end of 12-month follow-up, the cumulative incidence of viral suppression was 58.9% for DTG, 49.6% for C-EFV and 44.9% for H-EFV; the cumulative incidence of switching ART regimen was 4.1% for DTG, 10.0% for C-EFV and 5.7% for H-EFV; and the cumulative incidence of loss to program or death was 23.4% for DTG, 28.6% for C-EFV and 28.8% for H-EFV (Table 2). When restricting to the 2079 patients who had VL ascertained in the 12 months after tuberculosis diagnosis, the cumulative incidence of viral suppression was 90.7% for DTG, 79.5% for C-EFV and 80.3% for H-EFV. Median time until viral suppression was about 6 months for all groups and differences in viral suppression between DTG and EFV groups emerged just before this time (Figure 3). Cumulative incidence of viral suppression by exposure group was similar in magnitude among subgroups (Table 3). In multivariable regression, DTG was associated with significantly greater hazards of viral suppression compared with the C-EFV (adjusted subdistribution hazard ratio [aSHR] 1.28, 95% CI: 1.08-1.51) and H-EFV (aSHR 1.46, 95% CI: 1.28-1.67) groups     Abbreviations: ART, antiretroviral therapy; C-EFV, contemporaneous efavirenz; CI confidence interval; DTG, dolutegravir; H-EFV, historical efavirenz; HRZE, isoniazid, rifampicin, pyrazinamide and ethambutol. a Analyses stratified by recent viral load among those initiating ART >6 months before tuberculosis diagnosis are presented in Table S6. b Unable to estimate. ( Table 4). Hazard ratios had the same direction and were similar in magnitude when limited to patients with VL ascertained and by subgroup, with some differences in statistical significance.

Table 2. Crude cumulative incidence of viral suppression and competing events during 12-month follow-up for dolutegravir and efavirenz exposure groups
Results were similar with the main analysis when redefining viral suppression as <400 copies/ml (Tables S2 and S3) and when stratifying by the number of VL tests in the 12 months after tuberculosis diagnosis (Tables S4 and S5). When stratifying by most recent baseline VL among patients initiating ART >6 before tuberculosis diagnosis (Tables S6 and S7), differences between DTG and EFV groups appeared to be driven by those with a VL ≥1000 copies/ml or no VL test. Viral suppression was similar by exposure group for those with a recent baseline VL <1000 copies/ml.

D I S C U S S I O N
In a broad sample of HIV clinics in sub-Saharan Africa, >95% of sites reported prescribing dolutegravir-containing regimens to PWH receiving rifampicin as part of tuberculosis treatment and 90% of these sites reported using twice-daily dosing of dolutegravir to counteract the drug-drug interaction. Dolutegravir is being widely rolled out as a once-daily fixed dose combination tablet with tenofovir disoproxil fumarate and lamivudine ("TLD") [3]. Therefore, national programs need to acquire 50 mg tablets and dispensaries need to stock them to accommodate twice-daily dosing. Among sites using twice-daily dosing, >95% reported having dolutegravir 50 mg tablets available.
In the cohort study, a large proportion (91%) of patients receiving dolutegravir who had VL ascertained in the 12 months after tuberculosis diagnosis had viral suppression, which was lower (59%) for the entire sample that fully considered loss to program or death, which could preclude VL testing, and patients who did not have VL testing for other reasons. For both samples, dolutegravir was significantly associated with improved viral suppression compared with efavirenz. When stratifying by subgroup, there were some differences in statistical significance for comparisons, but overall, results were similar in magnitude. In the INSPIR-ING trial, 48-week viral suppression (<50 copies/ml) was similar in magnitude for both the dolutegravir (75%) and efavirenz (82%) arms among participants newly initiating ART; however, this trial was not powered to statistically compare viral suppression between treatment arms [16]. Real-world evidence from Botswana [27] and France [28] supports similar virologic effectiveness of dolutegravir compared with efavirenz among patients with tuberculosis co-infection receiving rifampicin.
The finding that viral suppression with dolutegravir was at least as good as (and possibly better) compared with efavirenz is supportive of HIV treatment programs already routinely prescribing dolutegravir to patients with tuberculosis co-infection. In some settings, efavirenz remains preferred for patients initiating ART at the time of tuberculosis diagnosis to avoid the drug-drug interaction with rifampicin [29] and our results support that it remains a reasonable alternative.
Our study provides reassurance about the virologic effectiveness of dolutegravir in the context of this drug-drug interaction and supports further expanding access to PWH in accordance with international guidelines, including those initiating rifampicin as part of tuberculosis treatment [1,2]. Despite these positive findings, the high proportion of patients who were lost to program or died, regardless of ART regimen, emphasizes the need to further improve outcomes among PWH who have tuberculosis co-infection.
The results from our cohort study should be interpreted in the context of some limitations. We attempted to adjust for potential confounders in regression analyses, which we considered to be patient characteristics that were significantly different between exposure groups. Nevertheless, because of the observational study design, unobserved confounders may be present. The comparison of DTG with H-EFV allowed for potentially less selection bias than the comparison with C-EFV, as dolutegravir was not yet available when these patients had a tuberculosis diagnosis. However, follow-up in the H-EFV group began as early as 2015 and thus, the lower viral suppression in this group may have been related to changes in VL testing availability and practices over time, including the use of targeted rather than routine VL monitoring [30]. Despite this, associations were generally similar between DTG and both C-EFV and H-EFV groups.
As we leveraged routine clinical data, misclassification of some variables and missing data related to erroneous or incomplete documentation is anticipated. For the inclusion criteria, it may be possible that a tuberculosis diagnosis was incorrectly documented. It may also be possible that some patients had drug resistant tuberculosis and were not receiving rifampicin; however, such treatment is often provided offsite in our setting [31]. To examine these potential sources of bias, we conducted subgroup analyses limited to those with documentation of HRZE and found that results were consistent with the main analysis.
We did not have information on dosing frequency of antiretroviral drugs, so we could not compare outcomes by dolutegravir dosing. Few patients in the DTG group were at sites that reported not using twice-daily dosing, precluding a robust subgroup analysis. The necessity of dolutegravir 50 mg twice daily for all patients receiving concomitant rifampicin remains unresolved [27,32,33]; however, further evidence is anticipated from an ongoing randomized trial [34]. Genotypic resistance testing would have allowed an assessment of resistance among patients with viral non-suppression on dolutegravir, as emergent dolutegravir resistance in the context of the drug-drug interaction with rifampicin has been described [35,36]. We also did not have data about safety or tolerability, precluding an assessment of risks versus benefits.

C O N C L U S I O N S
We documented the widespread programmatic implementation of dolutegravir for patients with tuberculosis co-infection at HIV clinics in sub-Saharan Africa and use of the recommended twice-daily dosing to counteract the drug-drug interaction with rifampicin. Despite this more complex regimen, dolutegravir did not negatively impact viral suppression.

C O M P E T I N G I N T E R E S T S
The authors declare that they have no competing interests.

A U T H O R S ' C O N T R I B U T I O N S
MLR and DN conceived the study. MLR, EB, MY, LF, KKW-K, NSS and DN contributed to the study design. EB, DM-N, RDW, CS-W, CC, WRM, GM, CK, TT, JAM, PL, AD, CT, IR, OCE and LD contributed to data collection. MLR analysed the data and wrote the manuscript. All authors participated in the interpretation of the results, revision of the manuscript, and have read and approved the final manuscript. http://onlinelibrary.wiley.com/doi/10.1002/jia2.25961/full | https://doi.org/10.1002/jia2.25961

A C K N O W L E D G E M E N T S
We would like to thank Fernanda Maruri (Vanderbilt University Medical Center) for coordinating the site survey, the members of the IeDEA working groups (Data Harmonization, Site Assessment, Tuberculosis and Lung Health) and the site investigators, clinicians and administrative staff who completed the survey.

F U N D I N G
The International Epidemiology Databases to Evaluate AIDS (IeDEA) is supported by the U.S. National Institutes of Health's National Institute of Allergy and Infectious Diseases, the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the National Cancer Institute, the National Institute of Mental Health, the National Institute on Drug Abuse, the National Heart, Lung, and Blood Institute, the National Institute on Alcohol Abuse and Alcoholism, the National Institute of Diabetes and Digestive and Kidney Diseases, the Fogarty International Center and the National Library of Medicine: Central Africa, U01AI096299; East Africa, U01AI069911; Southern Africa, U01AI069924; West Africa, U01AI069919. Informatics resources are supported by the Harmonist project, R24AI24872.

D I S C LO S U R E
This work is solely the responsibility of the authors and does not necessarily represent the official views of the U.S. National Institutes of Health.

D ATA AVA I L A B I L I T Y S TAT E M E N T
The data that support the findings of this study are available from the corresponding author upon reasonable request. Individuals who wish to request access to data from the IeDEA consortium for research purposes may submit a concept proposal, which is detailed at https://www.iedea.org/.

S U P P O R T I N G I N F O R M AT I O N
Additional information may be found under the Supporting Information tab for this article: Appendix S1. Members of the contributing IeDEA regions. Appendix S2. Site survey of dolutegravir use among patients with tuberculosis co-infection. Supplemental Table 1. Characteristics of sites included in survey of dolutegravir use in tuberculosis co-infection.
Supplemental Table 2. Cumulative incidence of viral suppression redefining viral suppression from <1000 copies/mL to <400 copies/mL (sensitivity analysis). Supplemental Table 3. Hazards regression models for the associations between dolutegravir and efavirenz groups with viral suppression redefined from <1000 copies/mL to <400 copies/mL (sensitivity analysis). Supplemental Table 4. Cumulative incidence of viral suppression stratified by number of viral load tests in the 12 months after tuberculosis diagnosis (sensitivity analysis). Supplemental Table 5. Hazards regression models for the associations between dolutegravir and efavirenz groups stratified by number of viral load tests in the 12 months after tuberculosis diagnosis (sensitivity analysis). Supplemental Table 6. Cumulative incidence of viral suppression stratified by baseline recent viral load among patients initiating antiretroviral therapy >6 months before tuberculosis diagnosis (sensitivity analysis). Supplemental Table 7. Hazards regression models for the associations between dolutegravir and efavirenz groups stratified by baseline recent viral load among patients initiating antiretroviral therapy >6 months before tuberculosis diagnosis (sensitivity analysis).